Abstract B019: Systemic proteomic remodeling following nephrectomy in renal cell carcinoma

Abstract Background: Renal cell carcinoma (RCC) exerts widespread systemic effects that extend beyond the tumor microenvironment. However, how the removal of the primary tumor reshapes the circulating proteome remains largely undefined. Characterizing these changes may reveal biomarkers of immune recovery and mechanisms by which tumors disrupt systemic immune function. Methods: We profiled plasma from 16 RCC patients collected before and after nephrectomy using the SomaLogic SOMAscan 11k assay v5.0, which quantifies 11,000 proteins. Data were z-score normalized and scaled in R. Differential abundance was analyzed using paired t-tests with false discovery rate (FDR) correction. Pathway analysis was performed using the GSEA package. Protein-protein correlation networks were constructed using the igraph package, and global topological parameters (node degree, edge strength, and network density) were compared before and after nephrectomy. Results: Nephrectomy induced broad proteomic remodeling consistent with systemic homeostatic restoration. Differential abundance and pathway enrichment analysis identified 1,737 significantly altered proteins (FDR <0.05), with decreases in pathways and mediators of immune suppression following tumor removal. Network analysis demonstrated a reduction in extremes in protein-protein correlations, node degree, and interaction strength, indicating a loss of tumor-driven network polarization. Together, these results suggest that the presence of RCC disrupts protein co-regulation, which normalizes following tumor removal. Conclusions: Our findings demonstrate that RCC drives coordinated systemic proteomic dysregulation that is partially reversed after nephrectomy. The observed reduction in network extremes reflects a global remodeling of circulating protein interactions, providing insight into how tumors perturb systemic physiology. Plasma proteomics and network metrics may offer sensitive indicators of systemic immune recovery and potential biomarkers of post-surgical immune restoration. Citation Format: Stephanie Schwartz, Julia Walker, Vivien Moritz, Soki Kashima, Adebowale Adeniran, Fed Ghali, Patrick Kenney, Michael Hurwitz, David Braun. Systemic proteomic remodeling following nephrectomy in renal cell carcinoma [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Innovations in Kidney Cancer Research: From Molecular Insights to Therapeutic Breakthroughs; 2026 Mar 13-16; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(5_Suppl_2):Abstract nr B019.

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Journal
Cancer Research
Published
2026-03-13
DOI
https://doi.org/10.1158/1538-7445.kidney26-b019
Primary Topic
Renal cell carcinoma treatment
Type
article
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article

Abstract B019: Systemic proteomic remodeling following nephrectomy in renal cell carcinoma

Soki Kashima, Patrick Aloysius Kenney, Michael E. Hurwitz, Stephanie Elzer Schwartz et al.
Cancer Research
Renal cell carcinoma treatment
article

Abstract B019: Systemic proteomic remodeling following nephrectomy in renal cell carcinoma

Soki Kashima, Patrick Aloysius Kenney, Michael E. Hurwitz, Stephanie Elzer Schwartz, Fed Ghali, Vivien Moritz, Adebowale Adeniran, Julia Walker, David A. Braun
article en

Abstract

Abstract Background: Renal cell carcinoma (RCC) exerts widespread systemic effects that extend beyond the tumor microenvironment. However, how the removal of the primary tumor reshapes the circulating proteome remains largely undefined. Characterizing these changes may reveal biomarkers of immune recovery and mechanisms by which tumors disrupt systemic immune function. Methods: We profiled plasma from 16 RCC patients collected before and after nephrectomy using the SomaLogic SOMAscan 11k assay v5.0, which quantifies 11,000 proteins. Data were z-score normalized and scaled in R. Differential abundance was analyzed using paired t-tests with false discovery rate (FDR) correction. Pathway analysis was performed using the GSEA package. Protein-protein correlation networks were constructed using the igraph package, and global topological parameters (node degree, edge strength, and network density) were compared before and after nephrectomy. Results: Nephrectomy induced broad proteomic remodeling consistent with systemic homeostatic restoration. Differential abundance and pathway enrichment analysis identified 1,737 significantly altered proteins (FDR <0.05), with decreases in pathways and mediators of immune suppression following tumor removal. Network analysis demonstrated a reduction in extremes in protein-protein correlations, node degree, and interaction strength, indicating a loss of tumor-driven network polarization. Together, these results suggest that the presence of RCC disrupts protein co-regulation, which normalizes following tumor removal. Conclusions: Our findings demonstrate that RCC drives coordinated systemic proteomic dysregulation that is partially reversed after nephrectomy. The observed reduction in network extremes reflects a global remodeling of circulating protein interactions, providing insight into how tumors perturb systemic physiology. Plasma proteomics and network metrics may offer sensitive indicators of systemic immune recovery and potential biomarkers of post-surgical immune restoration. Citation Format: Stephanie Schwartz, Julia Walker, Vivien Moritz, Soki Kashima, Adebowale Adeniran, Fed Ghali, Patrick Kenney, Michael Hurwitz, David Braun. Systemic proteomic remodeling following nephrectomy in renal cell carcinoma [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Innovations in Kidney Cancer Research: From Molecular Insights to Therapeutic Breakthroughs; 2026 Mar 13-16; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(5_Suppl_2):Abstract nr B019.

Cancer ResearchVol. 86(5_Supplement_2)
Yale University (US), University of New Haven (US)
Openalex Percentile: Top 22%
Renal cell carcinoma treatment
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